Ultraviolet light stable polymeric compositions

ABSTRACT

Ultraviolet light stable polymeric resin compositions comprising an ultraviolet light degradable polymeric resin component and an effective ultraviolet light absorbing amount of a particulate metal titanate component.

This application is a division of application Ser. No. 347,191, filedMay 4, 1989 now U.S. Pat. No. 4,987,164, issued Jun. 22, 1991.

FIELD OF THE INVENTION

This invention relates to improved ultraviolet light stabilizedpolymeric resin compositions, and to a method for their preparation. Theinvention further relates to a novel means for improving the ultravioletlight stability of ultraviolet light degradable polymeric resinmaterials.

BACKGROUND OF THE INVENTION

It is widely known that ultraviolet light radiation, whether from anatural source such as the sun or an artificial source such as interiorlighting, can accelerate both the physical and chemical breakdown ordeterioration of various polymeric resin materials. For example, it isknown that polyolefin, acrylic, polycarbonate, polyvinylaromatic,polyester, polyamide and polyvinylchloride resin materials are allsusceptible, to one degree or another, to both physical and chemicaldegradation when exposed to ultraviolet light radiation.

To protect these polymeric resin materials against deleterious effectsof ultraviolet light radiation, a number of commercial ultraviolet lightabsorbing additive agents have been developed. In general, thesecommercial light absorbing agents will provide the stability desired inotherwise ultraviolet light degradable polymeric resin materials eitherby absorbing the ultraviolet light radiation directly or by harmlesslydissipating this particular light energy through intermolecular energyprocesses.

In the main, the most widely employed commercial ultraviolet lightabsorbing additive agents are organic in nature and generally can begrouped into five basic categories. These categories include (1)hydroxybenzophenones, (2) hydroxyphenylbenzotriazoles, (3) salicylates,(4) aryl substituted acrylates and (5) aminobenzoates While theseorganic additives function as ultraviolet light absorbents, they arecostly to produce and can add significantly to the cost of formulatedpolymeric resin materials containing them.

A less expensive commercially available material for use as anultraviolet light absorbing additive agent in certain types of polymericresin materials is the inorganic metal oxide, titanium dioxide. Its usefor such purposes is known from U.S. Pat. No. 4,619,957 wherein it isdisclosed that titanium dioxide is added to poly(vinylchloride) resinformulations not only to provide pigmentation in the formulations butalso to impart improved ultraviolet light stability to suchformulations. It further is disclosed in this patent that one problemwith the use of titanium dioxide for this purpose is that due to thehigh loadings required and the strong tinting strength of the titaniumdioxide, it is not possible to fabricate products from such resinformulations in colors other than white or light pastel colors. Toovercome this problem, the solution proposed in this patent is toreplace a portion of the titanium dioxide in such resin formulation withcertain ultraviolet light absorbing benzoate compounds.

According to the disclosures in the above patent, reduction of thetitanium dioxide levels in such resin formulations allows for themanufacture of fabricated products in darker shades or colors. The addedbenzoate compounds function to maintain the stability of the fabricatedproducts, formerly provided by the high levels of titanium dioxide,against degradation by ultraviolet light radiation.

Another drawback to the use of titanium dioxide is that this pigmentdoes not appear to be universally suited for use as an ultraviolet lightabsorbing additive agent in all ultraviolet light degradable polymericresins. For example, when added to ultraviolet light degradablepolyamides (e.g., nylons) as a delusterant, titanium dioxide is believedto act as a photosensitizer and, in effect, increases the rate ofphotodegradation of the polyamide particularly at the longer wavelengthsin the ultraviolet light resin. Thus, to provide ultraviolet lightstability to a polyamide containing titanium dioxide it is usualpractice to further add to the polyamide resin formulation a stabilizingcompound such as a manganese salt together with other additives such ashypophosphorous acids, phosphites, phosphates, and the like. Kirk-OthmerEncyclopedia of Chemical Technology, Vol. 16, page 81, 2ed. (1968).

It is clear from the above that ultraviolet light stabilized polymericresin compositions have been prepared from a wide variety of ultravioletlight degradable polymeric resin materials and ultraviolet lightabsorbing additive agents. However, a need still exists for ultravioletlight stabilized polymeric resin compositions that are more economicalto produce than those based on the use of the aforementioned organicultraviolet light absorbing agents and which compositions are notbothered by problems, such as those mentioned above, associated with theuse of inorganic ultraviolet light absorbing agents such as titaniumdioxide.

SUMMARY OF THE INVENTION

In accordance with the present invention, economical ultraviolet lightstable polymeric resin compositions are provided which comprise anultraviolet light degradable polymeric resin component and an effectiveultraviolet light absorbing amount of a particulate metal titanatecomponent. The metal titanate component of the ultraviolet light stablepolymeric resin compositions of this invention comprises at least onemetal titanate compound corresponding to the broad general formula M_(a)M'_(b) Ti_(c) O_(d) in which M and M' are different metals selected fromGroups Ia, IIa, IIb, IIIa, IIIb, IVa, IVb, Va, VIIb and VIII of thePeriodic Table of the Elements, and in which a is a number ranging fromabout 0.1 to about 15, b is a number ranging from 0 to about 15, c is anumber ranging from about 1 to about 25 and d is a number ranging fromabout 2.1 to about 55.

BRIEF DESCRIPTION OF THE DRAWING

FIG. 1 is a graphical illustration of the ultraviolet light stability ofthe compositions of the present invention when exposed to a source ofultraviolet light.

FIG. 2 is a graphical illustration of the diffuse reflectance spectrumfor the metal titanate, barium titanate, versus the diffuse reflectancespectrum for titanium dioxide.

DETAILED DESCRIPTION OF THE INVENTION

Broadly, the present invention relates to ultraviolet light stablepolymeric resin compositions comprised of an ultraviolet lightdegradable polymeric resin component and a particulate metal titanatecomponent capable of absorbing ultraviolet light of wavelengths of about400 nm and below. In general, the resin component of the resincompositions of this invention will comprise any thermosetting andthermoplastic ultraviolet light degradable polymeric resin materialcapable of being fabricated into products such as, for example,decorative and protective coatings, films and sheeting, and any otherproducts produced by way of any of the variously known molding,extrusion and calendering techniques.

Typically, the polymeric resin materials useful in preparing theultraviolet light stable polymeric resin compositions of this inventionwill comprise any of the well-known resin materials such as polyolefin,polyvinylaromatic, acrylic, polycarbonate, polyester, polyamide andpolyvinylhalide resins. All of these disclosed resin materials are knownto be susceptible to degradation, to one degree or another, upon beingexposed to ultraviolet light radiation.

Representative, but nonlimiting, examples of specific polymeric resinmaterials useful as the resin component in the ultraviolet light stablepolymeric resin compositions of this invention include polyolefin resinssuch as polyethylene and polypropylene and the like; polyvinylaromaticresins such as polystyrene and copolymers and terpolymers therefor, suchas poly(styrene-acrylonitrite) and poly(styrene-butadiene-acrylonitrile)and the like; acrylic resins such as poly(acrylic acid),poly(methacrylic acid), poly(methyl acrylate), poly(methyl methacrylate)and the like; polycarbonate resins such as those obtained either by thephosgenation of dihydroxy aliphatic and aromatic monomers such asethylene glycol, propylene glycol, bisphenol A (i.e.,4,4'-isopropylidene diphenol) and the like, or by the base catalyzedtransesterification of bisphenol A with diphenylcarbonate to producebisphenol A polycarbonate; polyester resins such as poly(ethyleneterephthalate), poly(butylene terephthalate) and the like; polyamideresins such as nylon-6, nylon-6,6 and the like; epoxy resins such aspoly(epichlorohydrin/bisphenol A) and the like, and esters thereof suchas the epoxy resin esters prepared by the esterification ofpoly(epichlorohydrin/bisphenol A) with a fatty acid, rosin acid, talloil acid or mixtures thereof; and phenolic resins such as those preparedby reaction of formaldehyde with phenol, resorcinol, cresol, xylenol,p-tert-butylphenol and the like.

Particularly useful ultraviolet light stable polymeric resincompositions of the present invention, however, are those polymericresin compositions wherein the polymeric resin component comprises apoly(vinylhalide) resin. Such preferred poly(vinylhalide) resins includepoly(vinylchloride) homopolymer resins as well as poly(vinylchloride)copolymer resins resulting from the copolymerization of vinyl chloridemonomer with a second monomer such as, for example, other unsaturatedhalogenated hydrocarbons, styrene and its halogenated derivatives, vinylesters and ethers, olefins, dienes, esters and other derivatives ofacrylic and methacrylic acids, and olefinic dicarboxylic acids andesters thereof. Representative examples of such copolymerizable secondmonomers or comonomers include vinylidene chloride, vinyl acetate, vinylisobutyl ether, ethylene, propylene, isoprene, butadiene, methylacrylate, methyl methacrylate and the like. Typically, commerciallyavailable poly(vinylchloride) copolymer resins can contain from about 2to about 20 weight percent of the copolymerized comonomer. A moredetailed description of poly(vinylchloride) homopolymer and copolymerresins useful as the polymeric resin component in the ultraviolet lightstabilized polymeric resin compositions of this invention can be foundin Kirk-Othmer, Encyclopedia of Chemical Technology, Volume 21, pp369-379 and pp 402-405, 2ed. (1968), the teachings of which areincorporated herein in their entirely by reference. Particularly usefulpoly(vinylchloride) resins for preparing the UV light stabilizedpolymeric resin compositions of this invention are the rigidpoly(vinylchloride) homopolymer resins.

In addition to the polymeric resin component described above, theultraviolet light stable polymeric resin compositions of this inventionalso contain an effective ultraviolet light absorbing amount of aparticulate metal titanate as an ultraviolet light stabilizingcomponent. In general, the particulate metal titanates useful inpreparing the polymeric resin compositions of this invention comprisethose metal titanates corresponding to the broad general formula M_(a)M'_(b) Ti_(c) O_(d). With regard to this general formula, M and M'different metals selected from Groups Ia, IIa, IIb, IIIa, IIIb, IVa,IVb, Va, VIIb and VIII of the Periodic Table of the Elements and a is anumber ranging from about 0.1 to about 15, b is a number ranging from 0to about 15, c is a number ranging from about 1 to about 25 and d is anumber ranging from about 2.1 to about 55. The metal titanatescorresponding to this broad general formula further are characterized inthat each of the

metals M and M' as well as Ti (titanium) are in their most stableoxidation state and O (oxygen) is in stoichiometric balance with each ofM, M' and Ti such that the overall charge of these titanates is zero.

In a more preferred embodiment of this invention, the particulate metaltitanates found to provide particularly stable polymeric resincompositions include those metal titanates corresponding to the abovebroad general formula wherein the subscript "b" is zero. In thispreferred embodiment, the particulate metal titanates useful in thisinvention can be represented by the general formula M_(a) Ti_(c) O_(d)wherein M, a, c and d have the same meanings and values and thecompounds themselves the same characteristics as disclosed immediatelyabove. However, the most useful titanate compounds corresponding to theformula M_(a) Ti_(c) O_(d) are those wherein M is a metal selected fromGroups Ia, IIa and IIIa of the Periodic Table of the Elements andspecifically, the metals sodium, potassium, calcium, strontium, bariumand aluminum belonging to these Groups, a is a number ranging from 1 to2, c is a number ranging from 1 to 2 and d is a number ranging from 3 to5.

In general, the metal titanates corresponding to the above generalformulae and useful in the preparation of the ultraviolet light stablepolymeric resin compositions of this invention can be prepared by knowntechniques. For instance, these metal titanates can be prepared by firstforming a reactive mixture of one or more oxides, hydroxides orcarbonates of one or more of the above identified metals with a reactivetitanium compound such as titanium dioxide in any desired proportionsand then heating the mixture to elevated temperatures and maintainingthe mixture at such elevated temperatures until reaction of theingredients in the mixture to the desired metal titanate is achieved. Anexample of one such method for preparing metal titanates in this manneris the method described in U.S. Pat. No. 2,140,236 for preparingtitanates of metals of Groups Ia and IIa of the Periodic Table of theElements, i.e., titanates of the alkali and alkaline earth metals. Metaltitanates corresponding to the above general formulae also can beprepared by sintering or fusing together one or more oxides of one ormore of the above defined metals with titanium dioxide. The preparationof aluminum titanate, as disclosed herein, can be performed in thismanner. (Kirk-Othmer, Encyclopedia of Chemical Technology, Volume 20,page 413, 2ed. (1968)).

Particularly useful metal titanates corresponding to the above generalformulae include the meta-, di-, tri-and ortho-titanates of the metalslithium, sodium, potassium, calcium, barium, strontium and aluminum andboth chemical and physical mixtures thereof. Specific representative,but nonlimiting, examples of such particularly useful metal titanatesinclude lithium metatitanate (Li₂ TiO₃), lithium dititanate (Li₂ Ti₂O₅), lithium orthotitanate (Li₄ TiO₄), sodium metatitanate (Na₂ TiO₃),sodium dititanate (Na₂ Ti₂ O₅), sodium titanate (Na₂ Ti₃ O₇), potassiummetatitanate (K₂ TiO₃), potassium dititanate (K₂ Ti₂ O₅), calciummetatitanate (CaTiO₃), strontium metatitanate (SrTiO₃), bariummetatitanate (BaTiO₃) and aluminum metatitanate (Al₂ TiO₅) and bothchemical and physical mixtures thereof. Of the above representativemetal titanates the calcium, strontium, barium and aluminum titanateshave been found to be especially well suited to preparing the stablepolymeric resin compositions of this invention. All are obtained aswhite products, all have indexes of refraction less than titaniumdioxide (and thus scatter light less efficiently than titanium dioxide)and all absorb ultraviolet light radiation at wavelengths of 400 nm orbelow.

Typically, the size range of the above described particulate metaltitanates will be from about 0.01 to about 10 microns in diameter.Preferably, these particulate metal titanates will range in size fromabout 0.1 to about 1.0 microns in diameter.

As disclosed above, the polymeric resin compositions of this inventionwill comprise a polymeric resin component and an effective ultravioletlight stabilizing amount of the herein described particulate metaltitanates. Typically, these polymeric resin compositions will containfrom about 0.1 to about 25 weight percent and preferably from about 2 toabout 20 weight percent of the particulate metal titanate based on 100parts by weight of the polymeric resin component in the polymeric resincompositions. With particular regard to the above describedpoly(vinylchloride) resins it surprisingly has been found that whilethese amounts provide substantially the same degree of ultraviolet lightstability as equivalent amounts of pigmentary titanium dioxide, the useof the particulate metal titanate does not give rise to theaforementioned drawback associated with the use of pigmentary titaniumdioxide. That is, when a particulate metal titanate as defined herein isincorporated into a poly(vinylchloride) resin to form a polymeric resincomposition of this invention, significantly darker shades or colors canbe attained compared to poly(vinylchloride) resin compositionscontaining an equivalent amount of titanium dioxide and colorant.Utilizing the particulate metal titanates as defined herein, it also ispossible to obtain the same lighter shades or colors as in polymericresin compositions containing pigmentary titanium dioxide, but atsubstantially lower concentrations of the colorant.

The ultraviolet light stable polymeric resin compositions of thisinvention further can contain other conventional additives known in thisart. Representative, but nonlimiting, examples of such conventionaladditives include thermal stabilizers, impact modifiers, lubricants orprocessing acids, fillers, both organic and inorganic color pigments andplasticizers. These ingredients can be incorporated into the polymericresin compositions by conventional blending techniques includingmilling, Banbury or dry powder mixing techniques.

As mentioned hereinabove, particularly useful ultraviolet light stablepolymeric resin compositions of the present invention are those resincompositions preferably containing a poly(vinylchloride) resin as thepolymeric resin component. Such poly(vinylchloride) resin compositions,containing the particulate metal titanates as disclosed herein either ascomplete or partial replacements for the more commonly employed titaniumdioxide, exhibit excellent stability during processing and excellentultraviolet light stability upon exposure to a source of ultravioletlight radiation such as the sun.

The following examples are intended to illustrate the preparation of thepolymeric resin compositions of the present invention and theirstability upon exposure to a source of ultraviolet light. In theseexamples all parts and percentages are by weight unless otherwisespecified.

EXAMPLE 1

An ultraviolet light stable polymeric resin composition of the presentinvention was prepared by dry

blending 4.5 parts of barium titanate (B_(a) TiO₃), 4.5 parts oftitanium dioxide (TiO₂) and 100 parts of a poly(vinylchloride) sidingformulation. This siding formula was comprised of 90 parts of a rigidpoly(vinylchloride) resin, 1.34 parts of Thermolite T137, a tin basedthermal stabilizer available from M & T Chemicals, Inc., 1.12 parts ofcalcium stearate, 0.9 parts of Hostalub XL165, a lubricant availablefrom the Hoeschst Celanese Corporation, 1.34 parts of K120N Acryloid, aprocessing aid available from Rohm & Haas Company and 5.3 parts ofchlorinated polyethylene.

The dry blended mixture then was introduced into a Brabender plastographmixer wherein it was kneaded into a plastic dough at a rotational speedof 120 rpm and a temperature of 180° C. over a period of seven minutes.No evidence of degradation of the poly(vinylchloride) resin in theplastic dough thus produced was observed.

The plastic dough then was hot pressed into a number of rigid sheetshaving dimensions of 3.5×6×0.04 inches. Each of the sheets was producedat a temperature of about 193° C. and a ram pressure in the range offrom about 30,000 to about 35,000 psig over a period of about oneminute. The sheets, when removed from the press, were visually observedto be nearly white in color indicating that no degradation of thepoly(vinylchloride) resin in the sheets had taken place.

EXAMPLE 2

A second ultraviolet light stable polymeric resin composition wasprepared employing the identical procedures and substantially the sameingredients as employed in Example 1. The single exception was that inthis Example 2, 4.5 parts of calcium titanate (CaTiO₃) was employed inplace of the BaTiO₃ employed in Example 1.

The resulting dry blended mixture was kneaded into a plastic dough andthen hot pressed into a number of rigid sheets in the same identicalmanner as described above. Again, neither the plastic dough nor thepressed sheets exhibited signs of degradation of the poly(vinylchloride)resin contained therein.

EXAMPLE 3

A third ultraviolet light stable polymeric resin composition wasprepared employing the same identical procedures and substantially thesame ingredients as employed in Example 1. Again, the single exceptionwas that in this Example 3 strontium titanate (S_(r) TiO₃) was employedin place of the BaTiO₃.

The dry blended mixture again was kneaded into a plastic dough in theBrabender plastograph and the dough finally hot pressed into rigidsheets having the above described dimensions. Neither the dough nor thepressed sheets exhibited signs of degradation of the poly(vinylchloride)resin contained therein.

To test the ultraviolet stability of the polymeric resin compositionsprepared in Examples 1 through 3 above, the rigid sheets molded fromthese resin compositions were subjected to the accelerated QUVweathering test. For purposes of comparison, a rigid test sheet moldedfrom the same base poly(vinylchloride) siding formulation as employed inExamples 1 through 3 above but without any metal titanate or titaniumdioxide pigment having been added thereto also was prepared andsubjected to the accelerated QUV test. Utilizing this test, theultraviolet light stability of the polymeric resin compositions ofExamples 1 through 3 and of the base siding formulation were quicklydetermined by measuring the increase in the yellowness of the rigidsheets prepared therefrom with time. Any increase in the yellowness ofthe rigid test sheets indicates degradation of the resin compositioncontained in the sheets to be occurring. The results are graphicallyillustrated in FIG. 1. From FIG. 1 it can be seen that the rigid testsheets prepared from the resin compositions of Examples 1 through 3exhibit a significantly decreased rate of yellowing (i.e., degradation)compared to the rigid test sheet formed from the base siding formulationalone. This decreased rate continues over many hundreds of hours ofexposure to the ultraviolet light source and indicates that the resincompositions of Examples 1 through 3 possessed excellent resistance toattack by ultraviolet light.

As is clear from the above description, each of the siding formulationsof Examples 1 through 3 above contained, in addition to the particularmetal titanate identified, a quantity of titanium dioxide which is knownto be an ultraviolet light absorbing material. To demonstrate theultraviolet light absorbing capabilities of the metal titanatesthemselves, a series of powder samples was prepared in which each samplecontained 4 percent by weight of one of the metal titanates employed inthe Examples above and 4 percent by weight of a titanium dioxidepigment. In each instance, the remainder of the sample comprisedmagnesium dioxide as an inert carrier or matrix material. A referencesample comprised of only the titanium dioxide pigment and the inertmatrix material also was prepared. Each of the samples, including thereference sample, then was exposed to a source of ultraviolet lightradiation and the diffuse reflectance generated by each sample measuredand recorded. Referring to FIG. 2, which is the diffuse reflectancespectrum for the sample containing barium titanate (B_(a) TiO₃), it isplainly evident that the presence of the barium titanate provided asignificant decrease in diffuse reflectance compared to the referencesample containing only the titanium dioxide. The magnitude of thedecrease can be attributed solely to the ultraviolet absorbingcapability of the barium titanate itself. Decreases in diffusereflectance also were observed for the samples containing the calciumtitanate (CaTiO₃) and strontium titanate (SrTiO₃), respectively. Theobserved decrease in the diffuse reflectance of the samples containingthe metal titanates demonstrates the ultraviolet light absorbingcapability of these materials and thus the benefit to be gained by theiruse in the polymeric resin compositions of the present invention.

While the present invention has been described in terms of what areconsidered to be the preferred embodiments, it is to be understood thatchanges may be made thereto without departing from the spirit and scopethereof.

We claim:
 1. Ultraviolet light stable polymeric resin compositions comprising:at least one ultraviolet light degradable polymeric resin component; and an effective ultraviolet light absorbing amount of at least one particulate metal titanate component corresponding to the general formula

    M.sub.a M'.sub.b Ti.sub.c O.sub.d

in which M and M' represent different metal selected from Groups Ia, Ib, IIa, IIb, IIIa, IIIb, IVa, Va, VIIb and VIII of the Periodic Table of the Elements, in which a is a number ranging from about 0.1 to about 15, b is a number ranging from 0 to about 15, c is a number ranging from about 1 to about 25 and d is a number ranging from about 2.1 to about 55, in which M, M' and Ti are present in said titanate in their most stable oxidation state and O is in stoichiometric balance with M, M' and Ti such that the metal titanate possesses a zero charge and in which said particulate metal titanate ranges in size from about 0.1 to about 1.0 micron in diameter and absorbs ultraviolet light of wavelengths of about 400 nm and below.
 2. The stable polymeric resin compositions of claim 1 wherein the metals M and M' in said formula are metals selected from Groups Ia, IIa, IIb and IIIa of the Periodic Table of the Elements.
 3. The stable polymeric resin compositions of claim 2 wherein the metals M and M' in said formula are metal selected from the group consisting of lithium, sodium, potassium, magnesium, calcium, strontium, barium, zinc and aluminum.
 4. The stable polymeric resin compositions of claim 1 where in said general formula ranges from about 1 to about 2, b equals 0, c ranges from about 1 to about 2 and d ranges from about 3 to about
 5. 5. The ultraviolet light stable polymeric resin compositions of claim 1 wherein the effective ultraviolet light absorbing amount of said metal titanate component ranges from about 0.1 to about 25 weight percent based upon 100 parts by weight of said degradable polymeric resin component.
 6. The stable polymeric resin compositions of claim 1 wherein the ultraviolet light degradable polymeric resin component is selected from the group consisting of polyolefins, polyvinylaromatic, acrylic, polyamide, epoxy, phenolic polycarbonate, polyester and polyvinylhalide resins.
 7. The stable polymeric resin compositions of claim 6 wherein the ultraviolet light degradable polymeric resin component is selected from the group consisting of polyethylene, polypropylene, polystyrene and poly(vinylchloride) resins.
 8. The stable polymeric resin compositions of claim 7 wherein the ultraviolet light degradable polymeric resin component is a poly(vinylchloride) resin.
 9. The stable polymeric resin compositions of claim 1 wherein said resin compositions are in the form of a coating, a film, a sheet or a molded or extruded article.
 10. Ultraviolet light stable polymeric resin compositions comprising:at least one ultraviolet light degradable polymeric resin component selected from the group consisting of polyolefins, polyvinylaromatic and polyvinylhalide resins; and from about 0.1 to about 25 weight percent based on the weight of said polymeric resin of at least one particulate metal titanate component corresponding to the formula M_(a) Ti_(c) O_(d) wherein M is a metal selected from Groups Ia, IIa, IIb and IIa of the Periodic Table of the Elements, a is a number ranging from about 1 to about 2, c is a number ranging from about 1 to about 2 and d is a number ranging from about 3 to about 5, wherein both M and Ti are present in said titanate in their most stable oxidation state and O is in stoichiometric balance with M and Ti such that said titanate possesses a zero charge and wherein said titanate ranges in size from about 0.1 to about 1.0 micron in diameter and absorbs ultraviolet light of wavelengths of about 400 nm and below.
 11. The stable polymeric resin compositions of claim 10 wherein M is said formula is selected form the group consisting of lithium, sodium, potassium, magnesium, calcium, stronitum, barium, zinc and aluminum.
 12. The stable polymeric resin compositions of claim 10 wherein said ultraviolet degradable polymeric resin components is selected from the group consisting of polyethylene, polypropylene, polystyrene and poly(vinylchloride) resins.
 13. The stable polymeric resin compositions of claim 10 wherein said resin compositions are in the form of a coating, a film, a sheet or a molded or extruded article.
 14. The stable polymeric resin composition of claim 12, wherein said degradable polymeric resin component is poly(vinyl chloride) resin.
 15. Ultraviolet light stable polymeric resin compositions comprising:a polypropylene resin as an ultraviolet light degradable polymeric resin component; and from about 0.1 to about 25 weight percent based on the weight of said polymeric resin of a particulate metal titanate component corresponding to the formula M_(a) Ti_(c) O_(d) wherein M is a metal selected from Groups Ia, IIa, and IIIa of the Periodic Table of the Elements, a is a number ranging from about 1 to about 2, c is a number ranging from about 1 to about 2, and d is a number ranging from about 3 to about 5, wherein both M and Ti are present in said particulate titanate in their most stable oxidation state and o is in stoichiometric balance with M and Ti such that said particulate titanate possesses a zero charge and wherein said particulate titanate further is characterized as being comprised of particles ranges in size from about 0.01 to about 10 microns in diameter and capable of absorbing ultraviolet light of wavelengths of about 400 nm and below.
 16. Ultraviolet light stable polymeric resin compositions comprising:a polystyrene resin as an ultraviolet light degradable polymeric resin component; and from about 0.1 to about 25 weight percent based on the weight of said polymeric resin of a particulate metal titanate component corresponding to the formula M_(a) Ti_(c) O_(d) wherein M is a metal selected from Groups Ia, IIa, and IIIa of the Periodic Table of the Elements, a is a number ranging from about 1 to about 2, c is a number ranging from about 1 to about 2 and d is a number ranging from about 3 to about 5, wherein both M and Ti are present in said particulate titanate in their most stable oxidation state and o is in stoichiometric balance with M and Ti such that said particulate titanate possesses a zero charge and wherein said particulate titanate further is characterized as being comprised of particles ranges in size from about 0.01 to about 10 microns in diameter and capable of absorbing ultraviolet light of wavelengths of about 400 nm and below.
 17. A method for preparing ultraviolet light stable polymeric resin compositions comprising:providing at least one ultraviolet light degradable polymeric resin component; and combining said ultraviolet light degradable polymeric resin component with an effective ultraviolet light absorbing amount of at least one particulate metal titanate component corresponding to general formula M_(a) M'_(b) Ti_(c) O_(d) in which M and M' represent different metal selected from Groups Ia, Ib, IIa, IIb, IIIa, IIIb, IVa, Va, VIIb and VIII of the Periodic Table of the Elements, in which a is a number ranging from about 0.1 to about 15, b is a number ranging from 0 to about 15, c is a number ranging from about 1 to about 25 and d is a number ranging from about 2.1 to about 55, in which M, M' and Ti are present in said titanate in their most stable oxidation state and O is in stoichiometric balance with M, M' and Ti such that the metal titanate possesses a zero charge and in which said particulate metal titanate ranges in size from about 0.1 to about 1.0 micron in diameter and absorbs ultraviolet light of wavelengths of about 400 nm and below. 